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Safety and Efficacy of FURESTEM-AD Inj. for Moderate to Severe Atopic Dermatitis (AD) (smart(FURIN))

5. August 2021 aktualisiert von: Kang Stem Biotech Co., Ltd.

A Two-stage, Multi-center, Randomized, Double-Blind, Placebo Controlled, Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of FURESTEM-AD Inj. for Moderate to Severe Chronic Atopic Dermatitis

This clinical trial study is two-stage, multi-center, randomized, double-blind, placebo controlled, phase 3 clinical trial to evaluate the efficacy and safety of FURESTEM-AD Inj. for moderate to severe chronic atopic dermatitis.

Studienübersicht

Studientyp

Interventionell

Einschreibung (Voraussichtlich)

308

Phase

  • Phase 3

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studieren Sie die Kontaktsicherung

Studienorte

    • Jeollanam-do
      • Gwangju, Jeollanam-do, Korea, Republik von, 61453
        • Rekrutierung
        • Chosun University Hospital
        • Kontakt:
          • Chanho Na, professor

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

19 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  1. Adults aged 19 years and older at time of informed consent
  2. Subjects diagnosed with atopic dermatitis based on the Hanifin and Rajka diagnostic criteria
  3. Subjects with chronic atopic dermatitis that has been present for at least 1 year before screening
  4. Subjects with moderate to severe atopic dermatitis as indicated by:

    • EASI score ≥ 16 points at the time of screening and baseline (Day 1),
    • IGA score ≥ 3 points at the time of screening and baseline (Day 1), and
    • BSA affected by atopic dermatitis ≥ 10% at the time of screening and baseline (Day 1)
  5. Subjects who have documented history of insufficient response to stable use of atopic dermatitis treatment within 24 weeks before screening, or inability to receive such treatment because of safety issues
  6. Subjects who are willing to apply a stable dose of non-medicated topical moisturizer at least twice daily for at least 7 days before the baseline (Day 1) visit and the duration of the study
  7. Women of childbearing potential who use appropriate contraceptive methods during this trial period
  8. Subjects who have voluntarily agreed to participate in this trial in writing

Exclusion Criteria:

  1. Subjects with the following history of disease or surgery/procedure at screening

    1. Malignancy or lympho-proliferative disease within 5 years before screening (except completely treated carcinoma in situ of the cervix, or completely treated and resolved non-metastatic squamous or basal cell carcinoma of the skin)
    2. organ transplants
    3. History of mental illness, drug or alcohol abuse within 2 years before screening, as per Investigator's opinion
  2. Subjects with the following underlying disease at screening

    1. Chronic active, acute infection or superficial skin infections requiring treatment with systemic antibiotics, antivirals, antiparasitics, antiprotozoals or antifungals;
    2. Skin diseases, pigmentation, or extensive scarring other than atopic dermatitis that may affect the efficacy evaluations of the study
  3. Renal dysfunction with serum creatinine level > 2.0 mg/dL at screening
  4. Liver dysfunction with alanine aminotransferase (ALT) or aspartate aminotransferase (AST) levels exceeding 2.5 times the upper limit of the normal range (ULN) at the time of screening
  5. Subjects with the history of using leukotriene receptor antagonists, systemic steroids, phototherapy, systemic immunosuppressants/modulators including janus kinase (JAK) inhibitors, and/or any other systemic therapy (not mentioned in Exclusion Criteria 6 and 8) to treat atopic dermatitis or symptoms of atopic dermatitis (approved or off-label use) within 4 weeks before baseline (Day 1)
  6. Subjects with the history of using systemic or topical antihistamines, topical corticosteroids (TCS), topical calcineurin inhibitors (TCIs), or topical phosphodiesterase 4 (PDE4) inhibitors within 2 weeks before baseline (Day 1)
  7. Allergen immunotherapy within 6 months before baseline (Day 1)
  8. Subjects with the history of receipt of the following treatments before baseline (Day 1)

    1. B cell-depleting agents including rituximab within 6 months
    2. Other biologics including dupilumab within 5 half-lives (if known) or 12 weeks, whichever is longer
  9. Subjects with regular use (more than two times per a week) of a tanning booth/parlor within 4 weeks before screening visit
  10. Subjects with the history of a live (attenuated) vaccine injection within 12 weeks before baseline (Day 1) or the plan to inject a live (attenuated) vaccine within 24 weeks after randomization
  11. Subjects who are deemed to require prohibited concomitant medications drug/therapy during the study period
  12. Subjects with uncontrolled chronic disease that might require administration of oral corticosteroids such as uncontrolled and severe asthma
  13. Pregnant/lactating women and men and women of childbearing potential who plan to become pregnant or who refuse to use appropriate contraceptive methods during the study period
  14. Subjects with the history of receipt of any investigational products or devices from another clinical trial within 4 weeks or 5 half-lives (if known) pior to screening
  15. Positive serology for hepatitis B or C, or for HIV
  16. Subjects with prior use of FURESTEM-AD
  17. Subjects with history of anaphylaxis
  18. Subjects who are deemed to have difficulty in performing this study by the judgment of the Investigator and those with other medical findings that are unsuitable for participation in the study

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Vervierfachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Furestem-AD Inj.

Investigational product name: FURESTEM-AD® inj. 5.0 X 10^7 cells/1.5 mL

baseline (0week) Experimental group will receive Investigational product (FURESTEM-AD® inj. 5.0 X 10^7 cells/1.5 mL).

After 12 weeks, Experimental group will receive placebo.

the following study drug is injected respectively into both upper arms, both thighs, and abdomen (total of 5 regions)
the following study drug is injected respectively into both upper arms, both thighs, and abdomen (total of 5 regions)
Placebo-Komparator: Placebo

Placebo

baseline (0week) Placebo comparator group will receive placebo.

After 12 weeks, Placebo comparator group will receive Investigational product (FURESTEM-AD® inj. 5.0 X 10^7 cells/1.5 mL).

the following study drug is injected respectively into both upper arms, both thighs, and abdomen (total of 5 regions)
the following study drug is injected respectively into both upper arms, both thighs, and abdomen (total of 5 regions)

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
EASI(Eczema Area and Severity Index)-50
Zeitfenster: 12 weeks
Ratio of subject whose Eczema Area and Severity Index (EASI) decreased over 50% as contrasted with baseline value
12 weeks

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
EASI(Eczema Area and Severity Index)-75
Zeitfenster: 2,4,8,12 weeks
Ratio of subjects whose Eczema Area and Severity Index (EASI) decreased over 75% as contrasted with baseline value
2,4,8,12 weeks
EASI(Eczema Area and Severity Index)-50
Zeitfenster: 2,4,8 weeks
Ratio of subjects whose Eczema Area and Severity Index (EASI) decreased over 50% as contrasted with baseline value
2,4,8 weeks
EASI(Eczema Area and Severity Index) index
Zeitfenster: 2,4,8,12 weeks
Change and rate of change in Eczema Area and Severity Index (EASI) index as contrasted with baseline value
2,4,8,12 weeks
IGA(Investigator's Global Assessment) Score
Zeitfenster: 2,4,8,12 weeks
Proportion of subjects who Investigator's Global Assessment (IGA) score 0 or 1 and at least 2 points reduction in IGA score as contrasted with baseline value
2,4,8,12 weeks
SCORAD(SCORing Atopic Dermatitis)-50
Zeitfenster: 2,4,8,12 weeks
Ratio of subjects whose SCORing Atopic Dermatitis (SCORAD) decreased over 50% as contrasted with baseline value
2,4,8,12 weeks
SCORAD(SCORing Atopic Dermatitis) index
Zeitfenster: 2,4,8,12 weeks
Change and rate of change in SCORing Atopic Dermatitis (SCORAD) index as contrasted with baseline value
2,4,8,12 weeks
BSA(Body Surface Area)
Zeitfenster: 2,4,8,12 weeks
Change and rate of change in Body Surface Area (BSA) as contrasted with baseline value
2,4,8,12 weeks
Worst daily Pruritus NRS(Numerical Rating Scale)
Zeitfenster: 2,4,8,12 weeks
Rate of change in Worst daily Pruritus Numerical Rating Scale (NRS) as contrasted with baseline value
2,4,8,12 weeks
Average daily Pruritus NRS(Numerical Rating Scale)
Zeitfenster: 2,4,8,12 weeks
Rate of change in Average daily Pruritus Numerical Rating Scale (NRS) as contrasted with baseline value
2,4,8,12 weeks
Worst daily Pruritus NRS(Numerical Rating Scale) - 4 points
Zeitfenster: 2,4,8,12 weeks
Proportion of patients at least 4 points reduction in Worst daily Pruritus Numerical Rating Scale (NRS) as contrasted with baseline value
2,4,8,12 weeks
POEM(Patient-Oriented Eczema Measure)
Zeitfenster: 2,4,8,12 weeks
Change and rate of change in Patient-Oriented Eczema Measure (POEM) as contrasted with baseline value
2,4,8,12 weeks
DLQI(Dermatology Life Quality Index)
Zeitfenster: 2,4,8,12 weeks
Change and rate of change in Dermatology Life Quality Index (DLQI) as contrasted with baseline value
2,4,8,12 weeks
Rescue medicine
Zeitfenster: up to 12, 24 weeks
Total number of use and consumed amount of rescue medicine
up to 12, 24 weeks

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Yeonglib Park, professor (CI), Bucheon Hospital, Soonchunhyang University
  • Hauptermittler: Yangwon Lee, professor, Konkuk University Hospital
  • Hauptermittler: Sanguk Son, professor, Korea University
  • Hauptermittler: Bakrin Yoo, professor, Gangdong Kyunghee University Hospital
  • Hauptermittler: Jihyun Lee, professor, Seoul St. Mary'S Hospital
  • Hauptermittler: Donghoon Lee, professor, Seoul National University Hospital
  • Hauptermittler: Chanho Na, professor, Chosun University Hospital
  • Hauptermittler: Yooin Bae, professor, Hallym University Dongtan Seongsim Hospital
  • Hauptermittler: Hyunchang Ko, professor, Yangsan Pusan National University Hospital
  • Hauptermittler: Younghyun Jang, professor, Kyungpook National University Hospital
  • Hauptermittler: Jeongeun Kim, professor, The Catholic University of Korea Eunpyeong St. Mary's Hospital
  • Hauptermittler: Minkyung Shin, professor, KyungHee University Hospital
  • Hauptermittler: Sanghyun Cho, professor, Catholic University Incheon St. Mary's Hospital
  • Hauptermittler: Cheonuk Park, professor, Hallym University Gangnam Seongsim Hospital
  • Hauptermittler: Jooyeon Ko, professor, Hanyang University
  • Hauptermittler: Taeyoung Han, professor, Nowon Eulji University Hospital
  • Hauptermittler: Jiyoung Ahn, professor, National Medical Center

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

29. Juni 2021

Primärer Abschluss (Voraussichtlich)

1. Januar 2023

Studienabschluss (Voraussichtlich)

1. April 2023

Studienanmeldedaten

Zuerst eingereicht

4. Juli 2021

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

5. August 2021

Zuerst gepostet (Tatsächlich)

13. August 2021

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

13. August 2021

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

5. August 2021

Zuletzt verifiziert

1. Juli 2021

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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